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主营:分子类,蛋白类,抗体类,生化类试剂
℡ 4000-520-616
℡ 4000-520-616
Cell Technology/FAM-FMK/Poly Casp/FAM
产品编号:FAM
市  场 价:¥3700.00
场      地:美国(厂家直采)
产品分类: 抗体类>二抗>抗猫>
联系QQ:1570468124
电话号码:4000-520-616
邮      箱: info@ebiomall.com
美  元  价:$185.00
品      牌: Cell Technology
公      司:CellTechnology
公司分类:
Cell Technology/FAM-FMK/Poly Casp/FAM
商品介绍
  • Description
  • Additional Information
  • Readable Documents
  • Assay Principle
  • Reviews

Key Benefits

  • Non-cytotoxic assay arrests further apoptotic activity via caspase inhibition.
  • Cell permeablity permits direct visualization of cytosolic apoptotic events.
  • Apoptotic cell population does not diminish over time.
  • Add reagent directly to cells. No special buffer or media needed. No preparation of cell lysates required. Simple wash procedure.
  • Works in diverse cell lines: human, rodent, Drosophila.
  • Can be performed in conjunction with Annexin staining, TUNEL, antibody staining, or with other APO LOGIX reagents on the same population of cells.
  • Permits high through-put screening. Protocol can be adapted for ex vivo as well as in situ experiments.
  • Yields both quantitative and qualitative results. Gives strong signal with little background noise.
  • Mark activity across the range of caspase proteins. Poly-caspase and caspase-specific assays to target caspases 1, 2, 3, 6, 8, 9, or 10 are available.
  • Applications - Flow Cytometry, Fluorescence Plate Reader, Fluorescent Microscopy

Additional information

FAM

Poly Casp, Casp 3/7, Caspase 8 Detection, Caspase 9 Detection, Caspase 6 Detection, Caspase 1 Detection, Caspase 2 Detection, Caspase 10 Detection

Kit Size

25, 100

apop-1aapop-1bAPO LOGIX Carboxyfluoroscein Caspase Detection Kits label active caspases in living cells undergoing apoptosis. Cell Technology’s probes utilize carboxyfluorescein(FAM)-labeled peptide fluoromethyl ketone (FMK) caspase inhibitors (FAM-peptide-FMK). These FAM-peptide-FMK compounds are both cell permeable and non-cytotoxic during the course of the assay and thus allow the detection of active caspases in living cell systems.

Fig A. Jurkat cells treated with DMSO. Cells were labeled with FAM-VAD-FMK for 1 hour. Caspase activity was detected using flow cytometry.

Fig B. Jurkat cells treated with camptothecin. Cells were labeled with FAM-VAD-FMK for 1 hour. Caspase activity was detected using flow cytometry.

Document Title
FAMFMKProtocol
FAM-FMK Datasheet
msds.Apologix
TitleFileLinkAuthor(s)JournalYear; Edition:Pages
Granzyme B activates procaspase-3 which signals a mitochondrial amplification loop for maximal apoptosishttp://www.jcb.org/cgi/content/full/160/6/875Sunil S. Metkar, Baikun Wang, Michelle L. Ebbs,Jin H. Kim,Yong J. Lee, Srikumar M. Raja, Christopher J. FroelichJournal of Cell Biology, Volume 160, Number 62003; 875-885
Small-molecule XIAP inhibitors derepress downstream effector caspases and induce apoptosis of myeloid Leukemia cellshttp://www.bloodjournal.org/cgi/content/full/105/10/4043Carter, Gronda, Wang, et.alBlood, Vol 105, No 10May 2005; 4043-4050
Fenretinide enhances rituximab-induced cytotoxicity against B-cell lymphoma xenografts through a caspase dependant mechanismhttp://www.bloodjournal.org/cgi/content/full/103/9/3516Gopal, Pagel, et.alBlood, Vol 103, No 9May 2004; 3516-3520
http://www.nature.com/leu/journal/v19/n1/full/2403560a.html
Anoxia Is Necessary for Tumor Cell Toxicity Caused by a Low-Oxygen Environmenthttp://cancerres.aacrjournals.org/cgi/content/full/65/8/3171#FIG5Papandreou, Krishna, Kaper, et.alCancer Research 65April 15, 2005; 3171-3178
IFN-y Induces Apoptosis in Ovarian Cancer Cells in Vivo and in Vitrohttp://clincancerres.aacrjournals.org/cgi/content/full/9/7/2487Wall, Burke, Barton, Smyth, BalkwillClinical Cancer Research Vol. 9July 2003; 2487-2496
http://www.nature.com/onc/journal/v24/n24/full/1208542a.html
The removal of extracellular calcium: a novel mechanism underlying the recruitment of N-methyl-d-aspartate (NMDA) receptors in neurotoxicityhttp://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2005.03888.x?cookieSet=1Xin, Zhao, Gang, et.alEuropean Journal of Neuroscience, Vol 21, Issue 3Feb 2005; pp 622
Ligand-independent redistribution of Fas (CD95) into lipid rafts mediates clonotypic T cell deathhttp://www.nature.com/ni/journal/v5/n2/abs/ni1024.htmlJagan R Muppidi & Richard M SiegelNature Immunology 52004; 182-189
Attenuation of apoptosis in enterocytes by blocking potassium channelshttp://ajpgi.physiology.org/cgi/reprint/00001.2005v1.pdfLevitan, Makhina, et. alAm J Physiol Gastrointest Liver PhysiolJuly 14, 2005
Induction of Apoptosis Using Inhibitors of Lysophosphatidic Acid Acyltransferase-ß and Anti-CD20 Monoclonal Antibodies for Treatment of Human Non-Hodgkin"s Lymphomashttp://clincancerres.aacrjournals.org/cgi/content/abstract/11/13/4857John M. Pagel, Christian Laugen, Lynn Bonham, Robert C. Hackman, et.alClinical Cancer Research Vol. 11July 1, 2005; 4857-4866
Inhibition of PI3K, mTOR and MEK signaling pathways promotes rapid apoptosis in B-lineage ALL in the presence of stromal cell supporthttp://www.nature.com/leu/journal/v19/n1/abs/2403560a.htmlBertrand, Spengeman, Shelton, et.alLeukemia2005; 19, 98-102
Reference
Slee, E. A., C. Adrain, and S. J. Martin. 1999. Serial Killers: ordering caspase activation events in apoptosis. Cell Death and Differ. 6:1067-1074.
Walker, N. P., R. V. Talanian, K. D. Brady, L. C. Dang, N. J. Bump, C. R. Ferenz, S. Franklin, T. Ghayur, M. C. Hackett and L. D. Hammill. 1994. Crystal Structure of the Cysteine Protease Interleukin-1ß-Converting Enzyme: A (p20/p10)2 Homodimer. Cell 78:343-352
Wilson, K. P., J. F. Black, J. A. Thomson, E. E. Kim, J. P. Griffith, M. A. Navia, M. A. Murcko, S. P. Chambers, R. A. Aldape, S. A. Raybuck, and D. J. Livingston. 1994. Structure and mechanism of interleukin-1 beta converting enzyme. Nature 370: 270-275.
Rotonda, J., D. W. Nicholson, K. M. Fazil, M. Gallant, Y. Gareau, M. Labelle, E. P. Peterson, D. M. Rasper, R. Ruel, J. P. Vaillancourt, N. A. Thornberry and J. W. Becker. 1996. The three-dimensional structure of apopain/CPP32, a key mediator of apoptosis. Nature Struct. Biol. 3(7): 619-625.
Kumar, S. 1999. Mechanisms mediating caspase activation in cell death. Cell Death and Differ. 6: 1060-1066.
Thornberry, N. A., T. A. Rano, E. P. Peterson, D. M. Rasper, T. Timkey, M. Garcia-Calvo, V. M. Houtszager, P. A. Nordstrom, S. Roy, J. P. Vaillancourt, K. T. Chapman and D. W. Nicholson. 1997. A combinatorial approach defines specificities of members of the caspase family and granzyme B. Functional relationships established for key mediators of apoptosis. J. Biol. Chem. 272(29): 17907-17911.
Amstad, P.A., G.L. Johnson, B.W. Lee and S. Dhawan. 2000. An in situ marker for the detection of activated caspases. Biotechnology Laboratory 18: 52-56.
Bedner, E., P. Smolewski, P.A. Amstad and Z. Darzynkiewicz. 2000. Activation of caspases measured in situ by binding or fluorochrome-labeled inhibitors of caspases (FLICA): correlation with DNA fragmentation. Exp. Cell Research 259: 308-313.
Smolewski, P., E. Bedner, L. Du, T.-C. Hsieh, J. Wu, J. D. Phelps and Z. Darzynkiewicz. 2001. Detection of caspase activation by fluorochrome-labeled inhibitors: multiparameter analysis by laser scanning cytometry. Cytometry 44: 73-82.
Ekert, P. G., J. Silke and D. L. Vaux. 1999. Caspase inhibitors. Cell Death and Differ. 6:1081-1086.
Carcia-Calvo, M., E. Peterson, B. Leiting, R. Ruel, D. Nicholson and N. Thornberry. 1998. Inhibition of human caspases by peptide-based and macromolecular inhibitors. J. Biol. Chem. 273: 32608-32613.
Hirata, H., A. Takahashi, S. Kobayashi, S. Yonehara, H. Sawai, T. Okazaki, K. Yamamoto and M. Sasada. 1998. Caspases are activated in a branched protease cascade and control distinct downstream processes in Fas-induced apoptosis. J. Exp. Med. 187: 587-600.
Part#ReagentTemperature
Part# 302610X Wash Buffer2-8C
Part# 302710X Fixative2-8C
Part# 4013Propidium Iodide2-8C
Refer to Product DatasheetLyophilized FAM Labeled Peptide Inhibitor2-8C

Please select an ACF field to output

品牌介绍

Cell Signaling Technology (CST) 是一家由科学家创立的私营家族公司,致力于提供全球最高品质的创新研究和诊断产品,加速生物学认知以及实现个体化医疗。CST坚持自主生产和严格验证,其高质量的产品和专业的研发精神已被全球客户认可,被公认/票选为细胞信号研究的金标准、最佳抗体*、研究者的选择*、PTM(蛋白翻译后修饰)年度抗体公司*、十年抗体品牌*等(*来自CiteAb、LISA数据报告)。

CST提供最高品质的特色信号蛋白及磷酸化、甲基化、乙酰化、泛素化、SUMO化等翻译后修饰抗体,蛋白翻译后修饰筛选试剂盒及服务,还有偶联抗体,二抗,ChIP试剂盒,细胞因子,ELISA试剂盒,细胞检测试剂盒,蛋白实验配套试剂等,为您提供蛋白相关实验的一站式解决方案。


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